Quality Systems Engineer

Job description


  • Identify and implement effective QMS processes to support continuous improvement and lean initiatives onsite
  • You will be directly involved incoming inspection of materials and supplier quality management, overseeing general QA activity
  • Support and deliver continuous improvements and to employ problem solving tools including root cause analysis and CAPA identification. This will also involve taking a lead on the implementation of finding from CAPA and Root Cause Analysis to meet and exceed internal and external requirements
  • Conduct internal audits to ISO13485 and GMP requirements, addressing all NCR issues and preventing reoccurrence
  • Be part and take lead role in active improvement of the QMS while ensuring complete compliance to GMP for all devices



  • Minimum of 4-year experience in a medical device or similarly regulated environment with a science, engineering or equivalent degree
  • Good working knowledge of ISO13485 systems and medical device compliance


To apply for this position please contact James Porter at Sigmar Recruitment T: +353 91 455305 E:  

All applications will be treated with the strictest of confidence.  Sigmar will never forward your CV to a third party without prior consent